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Structure of 172648-19-0
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This boronate-bearing imidazopyridine derivative features a reactive methanol handle for Suzuki-Miyaura coupling, enabling efficient integration into complex heterocycles. The bromo substituent provides orthogonal functionality for further diversification. Bench-stable and moisture-tolerant, it streamlines access to bioactive scaffolds in medicinal chemistry.
(6-Bromo-3H-imidazo[4,5-b]pyridin-2-yl)methanol serves as a versatile building block for constructing imidazopyridine-based scaffolds in medicinal chemistry. The bromo group enables palladium-catalyzed cross-coupling reactions, while the pendant primary alcohol facilitates derivatization via esterification, etherification, or oxidation to aldehyde. Its bench-stable nature and compatibility with common protecting group strategies make it well-suited for multi-step synthesis of functionalized heterocycles.
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H302-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: